Evaluating subject-level incremental values of new markers for risk classification rule.

Pubmed ID: 23807696

Pubmed Central ID: PMC4527584

Journal: Lifetime data analysis

Publication Date: Oct. 1, 2013

Affiliation: Department of Biostatistics, Harvard University, Boston, MA, 02115, USA, tcai@hsph.havard.edu.

MeSH Terms: Humans, Female, Aged, Risk Factors, United States, Coronary Disease, Confidence Intervals, Statistics, Nonparametric, Risk, Antihypertensive Agents, C-Reactive Protein, Biostatistics, Biomarkers

Grants: HHSN268200800007C, HHSN268201200036C, N01HC55222, N01HC85079, N01HC85080, N01HC85081, N01HC85082, N01HC85083, N01HC85086, R01 AG023629, U01 HL080295, R21 HL085375

Authors: Cai T, Tian L, Lloyd-Jones D, Wei LJ

Cite As: Cai T, Tian L, Lloyd-Jones D, Wei LJ. Evaluating subject-level incremental values of new markers for risk classification rule. Lifetime Data Anal 2013 Oct;19(4):547-67. Epub 2013 Jun 27.

Studies:

Abstract

Suppose that we need to classify a population of subjects into several well-defined ordered risk categories for disease prevention or management with their "baseline" risk factors/markers. In this article, we present a systematic approach to identify subjects using their conventional risk factors/markers who would benefit from a new set of risk markers for more accurate classification. Specifically for each subgroup of individuals with the same conventional risk estimate, we present inference procedures for the reclassification and the corresponding correct re-categorization rates with the new markers. We then apply these new tools to analyze the data from the Cardiovascular Health Study sponsored by the US National Heart, Lung, and Blood Institute. We used Framingham risk factors plus the information of baseline anti-hypertensive drug usage to identify adult American women who may benefit from the measurement of a new blood biomarker, CRP, for better risk classification in order to intensify prevention of coronary heart disease for the subsequent 10 years.